Provide a stepwise synthesis for the following Provide a stepwise synthesis for the 28. 0HNO Н...
please answer and show work for stepwise synthesis and other questions. 1. Provide a stepwise synthesis for the dipeptide Ser-Phe. Draw all steps including protecting groups. H2N-CH-C-OH H2N-CH-C-OH CH2 Phe Ser 2. Using ethyl 3-methylbutanoate as your only source of carbon and using any other reagents necessary, propose a stepwise synthesis for the following conversion. 3. Provide the reagents necessary to carry out the following conversion. 4. Provide the structures of the products in each step of the following reaction...
(20) 2. Provide a stepwise synthesis for either of the following target molecules. If you provide correct syntheses for both a 20 bonus will be awarded. para-bromotoluene and diethyl malonate Br
Provide a stepwise synthesis for the following reaction. you may use the indicated starting materials as well as any organic or inorganic reagents.
79. Provide stepwise synthesis for the following HỊCO. 64. Predict the product for the following Diels-Alder reaction EU-UEU-UE
Provide a stepwise synthesis for the following compound using benzyl alcohol as you only source of carbon & using any other reagents necessary OH
9. Provide a stepwise synthesis to carry out the following conversions CN Br Br (a) (b) 2 но,S OH
7) Provide a stepwise synthesis for the following compound using benzyl alcohol as your only source of carbon and using any other reagents necessary. OH OH benzyl alcohol
9. Provide a stepwise synthesis to carry out the following conversions: CN Br (b) 2 HO,S -он
Provide the multistep synthesis for the following reaction. Include the reagnets. ОН Н Br Br
Please answer all components. Question 7 (15 points) Propose a stepwise synthesis for the following reaction. You may use any reagents and/or additional molecules that you wish Question 8 (15 points). Provide a stepwise synthesis for the following reaction. (There are multiple synthesis pathways)